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Respiratory Beta-Agonists

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Respiratory Beta-Agonists Therapeutic Class Overview Respiratory Beta-Agonists INTRODUCTION Respiratory beta2-agonists are primarily used to treat reversible airway disease. They are Food and Drug Administration (FDA)-approved for the treatment of asthma, chronic obstructive pulmonary disease (COPD), exercise-induced asthma/bronchospasm, and/or reversible bronchospasm. Asthma is a chronic lung disease that inflames and narrows the airways, making it difficult to breathe. Asthma causes recurring periods of wheezing, chest tightness, shortness of breath, and coughing. Asthma affects people of all ages, but most often starts during childhood. In the United States, more than 25 million people are known to have asthma, including about 7 million children. The exact cause(s) of asthma are unknown. A combination of factors such as genetics, certain respiratory infections during childhood, and contact with airborne allergens can contribute to its development. Most patients with asthma have allergies (National Heart, Lung, and Blood Institute [NHLBI] 2014). ○ Current pharmacologic options for asthma management are categorized as: (1) long-term control medications to achieve and maintain control of persistent asthma, and (2) quick-relief medications used to treat acute symptoms and exacerbations. ○ Long-term control medications for asthma include (NHLBI 2007): . Corticosteroids (inhaled corticosteroids [ICSs] for long-term control; short courses of oral corticosteroids to gain prompt control of disease, long-term oral corticosteroids for severe persistent asthma) . Cromolyn sodium and nedocromil . Immunomodulators (ie, omalizumab) . Leukotriene modulators . Long-acting beta2-agonists (LABAs) . Methylxanthines (ie, theophylline) ○ Quick-relief medications for asthma include (NHLBI 2007): . Anticholinergics (ie, ipratropium bromide), as an alternative bronchodilator for those not tolerating a short-acting beta2-agonist (SABA) . SABAs (therapy of choice for relief of acute symptoms and prevention of exercise-induced bronchospasm) . Systemic corticosteroids (not short-acting, but used for moderate and severe exacerbations) ○ In recent years, additional medications have been made available for select subsets of patients with asthma, including the interleukin-5 (IL-5) antagonists benralizumab, mepolizumab, and reslizumab, and the interleukin-4 (IL-4) antagonist dupilumab, for the management of severe asthma with an eosinophilic phenotype (Prescribing information: Cinqair 2018, Dupixent 2018, Fasenra 2017, Nucala 2017). Additionally, tiotropium, long used for COPD, has been FDA-approved for the treatment of asthma (Spiriva Respimat prescribing information 2018). ○ ICSs are the most effective, most commonly recommended long-term control medications used for the treatment of asthma. The LABAs should not be used as monotherapy for the management of asthma due to increased risk for serious adverse events, including death. However, they are effective adjunctive therapy in patients who are not adequately controlled with an ICS alone. Theophylline and mast-cell stabilizers have weak to low efficacy in asthma. Theophylline has an unfavorable side-effect profile and may be life-threatening at high doses. Mast-cell stabilizers have a more favorable safety profile. Tiotropium is an option for add-on therapy in patients ≥ 12 years old with a history of exacerbations. An IL-5 antagonist or the immunoglobulin E (IgE) antagonist, omalizumab, may be added if patients require a higher level of care. Omalizumab is used in patients with moderate to severe allergic asthma while IL-5 antagonists are used for severe eosinophilic asthma. SABAs are the medication of choice for the relief of bronchospasm during acute exacerbations of asthma (Fasenra prescribing information 2017, NHLBI 2007, Global Initiative for Asthma [GINA] 2018). COPD is characterized by persistent respiratory symptoms and airflow limitation due to airway and/or alveolar abnormalities. The abnormalities are usually caused by exposure to noxious particles or gases. Airflow limitation is caused by a combination of small airway disease (eg, obstructive bronchiolitis) and parenchymal destruction (emphysema); the relative contributions of each component vary between patients. The most common symptoms of COPD include dyspnea, cough, and sputum production (Global Initiative for Chronic Obstructive Lung Disease [GOLD] 2019). Data as of November 19, 2018 KS-U/CK-U/ALS Page 1 of 12 This information is considered confidential and proprietary to OptumRx. It is intended for internal use only and should be disseminated only to authorized recipients. The contents of the therapeutic class overviews on this website ("Content") are for informational purposes only. The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Patients should always seek the advice of a physician or other qualified health provider with any questions regarding a medical condition. Clinicians should refer to the full prescribing information and published resources when making medical decisions. ○ COPD affects 6.4% of the United States (U.S.) population and is the major contributor to mortality from chronic lower respiratory diseases, the third leading cause of death in the U.S. (Centers for Disease Control and Prevention 2017). Globally, COPD is the fourth leading cause of death and is expected to be the third leading cause of death by 2020; the burden of COPD continues to increase due to continued exposure to risk factors and aging of the population (GOLD 2019). ○ Cigarette smoking is the main risk factor for COPD; other risk factors include biomass fuel exposure (such as from cooking and heating in poorly ventilated dwellings) and air pollution. Host factors such as genetic abnormalities, abnormal lung development, and accelerated aging can predispose individuals to COPD development (GOLD 2019). ○ Patients with COPD may experience exacerbations, which are periods of acute worsening of respiratory symptoms (GOLD 2019). ○ Pharmacologic therapy for COPD can reduce symptoms, reduce the frequency and severity of exacerbations, and improve patients’ health status and exercise tolerance. There is no conclusive evidence that COPD medications modify the long-term decline in lung function characteristics of COPD (GOLD 2019). ○ Pharmacologic options for COPD treatment comprise several classes, including beta2-agonists, anticholinergics, methylxanthines, ICSs, various combination products, and the phosphodiesterase (PDE)-4 inhibitor, roflumilast. Pharmacologic treatments should be individualized based on symptom severity, risk of exacerbations, side effects, comorbidities, drug availability, and cost, as well as the patient’s response, preference, and ability to use various drug delivery devices (GOLD 2019). ○ Inhaled bronchodilators are central to COPD symptom management, and are usually given on a regular basis to prevent or reduce symptoms. Several long-acting inhaled bronchodilators are available, and use of short-acting bronchodilators on a regular basis is not generally recommended (GOLD 2019). ○ Beta2-agonists differ in their dosing requirements, pharmacokinetic parameters, and potential adverse effects. Several of the SABAs are available generically in at least 1 strength or formulation; however, there are no generic formulations for the LABAs. This review includes the single-agent inhaled and oral beta2-agonists. Although several agents are also available in combination inhalers along with an ICS or an anticholinergic, the combination products are not included in this review. ○ Tables in this review are organized by whether the drug product is short- or long-acting. Note that extended-release albuterol is categorized as short-acting for the purposes of this review, along with the other albuterol products. Medispan class/subclass: Respiratory sympathomimetics/beta adrenergics Table 1. Medications Included Within Class Review Drug Generic Availability Short-acting beta2-agonists (oral and inhaled) albuterol inhalation aerosols and powder - (ProAir HFA, ProAir RespiClick dry powder inhaler, Proventil HFA, Ventolin HFA) albuterol solution for nebulization albuterol, oral tablets, extended-release tablets, and syrup levalbuterol inhalation aerosol (Xopenex HFA and generic) -* levalbuterol solution for nebulization (Xopenex and generics) metaproterenol, oral tablets and syrup terbutaline, oral tablets and injection Long-acting beta2-agonists (inhaled) Arcapta Neohaler (indacaterol) inhalation powder - Brovana (arformoterol) solution for nebulization - Perforomist (formoterol) solution for nebulization† - Serevent Diskus (salmeterol) inhalation powder - Striverdi Respimat (olodaterol) inhalation spray - Abbreviations: HFA = hydrofluoroalkane *No A-rated generics have been approved by the FDA; however, an authorized generic is available. †Formoterol was previously available as a dry powder inhaler (Foradil Aerolizer); however, this formulation is no longer marketed. (Drugs@FDA 2018, Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations 2018) Data as of November 19, 2018 KS-U/CK-U/ALS Page 2 of 12 This information is considered confidential and proprietary to OptumRx. It is intended for internal use only and should be disseminated only to authorized recipients. The contents of the therapeutic class overviews on this website ("Content") are for informational purposes only. The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Patients should
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